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Movement Disorders : Official Journal of the Movement Disorder Society|February 17, 2023
Complex Ataxia-Dementia Phenotype in Patients with Digenic TBP/STUB1 Spinocerebellar AtaxiaLorenzo Nanetti, Stefania Magri, Mario Fichera, et al.
European Journal of Internal Medicine|July 2, 2025
Modulation of hypoxia-sensitive non-coding RNAs following continuous positive airway pressure therapy in obstructive sleep apnea in peripheral bloodFrancesco Fanfulla, Veronica Barbi, Tiziana Bachetti, et al.
Frontiers in Neurology|January 24, 2022
Multifaceted and Age-Dependent Phenotypes Associated With Biallelic <i>PNPLA6</i> Gene Variants: Eight Novel Cases and Review of the LiteratureLorenzo Nanetti, Daniela Di Bella, Stefania Magri, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Digenic inheritance of STUB1 variants and TBP polyglutamine expansions explains the incomplete penetrance of SCA17 and SCA48Stefania Magri, Lorenzo Nanetti, Cinzia Gellera, et al.
International Journal of Molecular Sciences|April 13, 2023
Effects of Human LAV-BPIFB4 Gene Therapy on the Epigenetic Clock and Health of Aged MiceMaria Elisa Giuliani, Veronica Barbi, Giorgia Bigossi, et al.
Journal of Neurology|December 6, 2018
ANO10 mutational screening in recessive ataxia: genetic findings and refinement of the clinical phenotypeLorenzo Nanetti, Elisa Sarto, Anna Castaldo, et al.
Human Molecular Genetics|January 11, 2022
Hsa-miR223-3p circulating level is upregulated in Friedreich's ataxia and inversely associated with HCLS1 associated protein X-1, HAX-1Andrea Quatrana, Elena Morini, Francesca Tiano, et al.
Cardiovascular Diabetology|July 3, 2025
Cardiometabolic heart failure with preserved ejection fraction: from molecular signatures to personalized treatmentEra Gorica, Martin A Geiger, Ludovica Di Venanzio, et al.
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